Dear Researchers,
I need a comprehensive guideline to follow to determine analysis cut-off points (e.g.: number of nuclei per sample, percentages to consider a deletion present, false +/- testing for each probe since the % of hybridisation is different for each probe).
I am using Leica: TP53, LEU1, +12 and ATM mutations for my FISH experiments. So far the only one I have found that is of any use is this:Article Guidance for Fluorescence in Situ Hybridization Testing in H...
Does anyone have any other papers that may be useful/helpful for my purpose? Would be better if it was specific to CLL.
Thanks in advance.